DOCUZEN

Manufacturer
Village Pharma | Pharbest Pharmaceuticals, Inc.
Effective date
2025-06-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:02:50

Label at a glance#

ProductDOCUZEN
Active ingredientSENNOSIDES, DOCUSATE SODIUM
Label structure9 sections

Indications and uses

• relieves occasional constipation (irregularity) • generally produces a bowel movement in 6-12 hours

Dosage and administration

• take preferably at bedtime or as directed by a doctor age starting dosage maximum dosage Adults and children 12 years and over 2 tablets once a day  4 tablets twice a day Children 6 to under 12 years 1 tablet once a day 2 tablets  twice a day Children 2 to under 6 years  1/2 tablet  once a day 1 tablet twice a day Children under 2 years ask a doctor ask a  doctor

Storage and handling

• each tablet contains 10 mg of calcium, sodium 5 mg • store at 25°C (77°F); excursions permitted between 15 o -30 o C (59 o -86 o F)

Label contents#

Full prescribing information#

Active Ingredients (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Sennosides from Senna Concentrate 8.6mg

Docusate Sodium 50mg

Purpose

OTC - PURPOSE SECTION

Laxative

Stool Softner

Uses

INDICATIONS & USAGE SECTION

  • relieves occasional constipation (irregularity)
  • generally produces a bowel movement in 6-12 hours

Warnings

WARNINGS SECTION

Do not use

  • laxative products for longer than 1 week unless directed by a doctor
  • if you are taking mineral oils, unlesss directed by a doctor

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • stomach pain
  • nausea
  • vomiting
  • noticed a sudden change in bowel habits that continues over a period of 2 weeks

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you have rectal bleeding 
  • you fail to have a bowel movement after the use of a laxative.

These may indicate a serious condition.

If pregnant or breast feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use. 

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • take preferably at bedtime or as directed by a doctor

age

starting dosage

maximum dosage

Adults and children 12 years and over

2 tablets once a day 

4 tablets twice a day

Children 6 to under 12 years

1 tablet once a day

2 tablets  twice a day

Children 2 to under 6 years 

1/2 tablet  once a day

1 tablet twice a day

Children under 2 years

ask a doctor

ask a  doctor

Other information

STORAGE AND HANDLING SECTION

  • each tablet contains 10 mg of calcium, sodium 5 mg
  • store at 25°C (77°F); excursions permitted between 15o-30oC (59o-86oF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

croscarmellose Sodium, D&C Yellow# 10, dicalcium phosphate, FD&C Yellow #6, magnesium stearate, microcrystalline cellulose, polyvinyl alcohol, polyethylene glycol, sodium benzoate, talc & titanium dioxide.

Questions or comments?

OTC - QUESTIONS SECTION

1-800-828-0464 Mon-Fri 8 AM to 4 PM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VillagePharma

NDC 71574-700-60

DOCUZEN

Sennosides 8.6mg &

Docusate Sodium 50mg

60 TABLETS

Manufactured in the USA

image of Label
image of Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
998740sennosides 8.6 MG / docusate sodium 50 MG Oral TabletPSN3
998740docusate sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSCD3
998740DOSS Sodium 50 MG / sennosides, USP 8.6 MG Oral TabletSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71574-700-602025-06-11C16284748780-1d6a99b39-4fac-a426-e053-dadaa90af4c2Drug Facts
71574-700-602025-01-30C16284748780-1d6a99b39-4fac-a426-e053-dadaa90af4c2Drug Facts
71574-700-602023-11-10C16284748780-1d6a99b39-4fac-a426-e053-dadaa90af4c2Drug Facts
71574-700-602022-01-28C16284748780-1d6a99b39-4fac-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71574-700-60DOCUZEN60 in 1 BOTTLE, PLASTICTABLET603

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71574-700-60EA - Each71574-700663e7d7f-3f91-4d2c-8cff-71d91c95393012019-01-24

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71574-70071574-700-60

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DOCUZENSENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MGVillage Pharma29102014-9b0e-4899-958d-83111f94a6122025-06-01WarningsExact identifier
ndc (package): 71574-700-60
ndc (product): 71574-700
ndc11 (package): 71574070060
spl id: bf899923-8769-4738-88ea-b1a07997b959
spl set id: 29102014-9b0e-4899-958d-83111f94a612

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.